Berna Seker Yilmaz

Employment

• Guy's and St Thomas' NHS Foundation Trust Consultant
  2024 - Present
• University College London Institute of Child Health Research Associate
  2019 - Present

Education

Education history is unavailable.

Projects & Funding

Projects & funding information is unavailable.

Publications (48)

• Harmonizing Perspectives on MPS II Care in Türkiye: A Delphi Study Towards Treatment Management Consensus
  Healthcare 2026 0 citations DOI: 10.3390/healthcare14091214
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• The Evolving Landscape of Fetal Therapy: Surgical Interventions and Emerging Biologics
  Biologics 2026 0 citations DOI: 10.3390/biologics6020011
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• Longitudinal outcomes of non-transplanted ornithine transcarbamylase deficiency in males and females: a multicentre UK natural history cohort
  Orphanet Journal of Rare Diseases 2026 0 citations DOI: 10.1186/s13023-026-04517-w
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• Developmental and Cognitive Outcomes in 342 Patients With Different Types of Hyperphenylalaninemia
  SiSli Etfal Hastanesi Tip Bulteni / The Medical Bulletin of Sisli Hospital 2025 0 citations DOI: 10.14744/semb.2025.09471
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• Safety and effectiveness of ataluren in patients with Duchenne muscular dystrophy: single-center experience from Saudi Arabia
  Journal of International Medical Research 2024 1 citation DOI: 10.1177/03000605241305252
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• Targeting the liver to treat the eye
  EMBO Molecular Medicine 2023 5 citations DOI: 10.15252/emmm.202217285
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• Expanding the phenotypic landscape of Gaucher disease type 3c with a novel entity - Transient neonatal cholestasis
  European Journal of Medical Genetics 2023 6 citations DOI: 10.1016/j.ejmg.2023.104764
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• AAV-mediated gene therapy for rare metabolic disorders: turning a promise into a reality
  The Biochemist 2023 0 citations DOI: 10.1042/bio_2023_128
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• Genetic Therapy Approaches for Ornithine Transcarbamylase Deficiency
  Biomedicines 2023 25 citations DOI: 10.3390/biomedicines11082227
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• Diagnostic and Management Issues in Patients with Late-Onset Ornithine Transcarbamylase Deficiency
  Children 2023 22 citations DOI: 10.3390/children10081368
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